Posted:12 hours ago|
Platform:
Work from Office
Full Time
1. To review the product manufacturing records, testing records.
2. To monitor the aseptic practices in the shifts like online process checking and documentation.
3. To co-ordinate for in-process sampling and to monitor the EM activities
4. Responsible for ensuring the Validation & Calibration activities.
5. Validation & Qualification protocols preparation, and the implementation
6. Preparation and Review of SOPs.
7. Responsibility of Sterile IPQA operations
8. Handling of the change controls and to ensure the implementation of changes
9. Preparation and Review of the quality risk assessment.
10. Responsible for ensuring the deviations and OOS are investigation and necessary corrective and preventive actions are implemented.
Gland Pharma
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